您的位置:山东大学 -> 科技期刊社 -> 《山东大学学报(医学版)》

山东大学学报(医学版) ›› 2015, Vol. 53 ›› Issue (5): 31-35.doi: 10.6040/j.issn.1671-7554.0.2015.047

• 基础医学 • 上一篇    下一篇

病毒性心肌炎小鼠调节性B细胞的变化

岑治宏, 郭予洁, 伍伟锋, 李丽萍, 周秋曦   

  1. 广西医科大学第一附属医院心内科, 广西 南宁 530021
  • 收稿日期:2015-01-13 修回日期:2015-04-01 出版日期:2015-05-10 发布日期:2015-05-10
  • 通讯作者: 伍伟锋。E-mail:wucna65@163.com E-mail:wucna65@163.com
  • 基金资助:
    国家自然科学基金(81450055)

Changes of regulatory B cells in mice with viral myocarditis induced by Coxsackie virus

CEN Zhihong, GUO Yujie, WU Weifeng, LI Liping, ZHOU Qiuxi   

  1. Department of Cardiology, First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi, China
  • Received:2015-01-13 Revised:2015-04-01 Online:2015-05-10 Published:2015-05-10

摘要: 目的 观察病毒性心肌炎小鼠不同时间点调节性B淋巴细胞(Breg)亚群的变化,探讨其在病毒性心肌炎发病中的作用。方法 将小鼠随机分为实验组和对照组,实验组腹腔注射柯萨奇病毒B3(CVB3),对照组注射等量磷酸盐缓冲液(PBS)。依据注射后的时间,实验组和对照组均设1周和2周时间点亚组。应用苏木素伊红染色后观察心肌病理改变并计算心肌病理积分,采用RT-PCR法检测心肌组织中CVB3 mRNA的表达水平,采用流式细胞术检测小鼠脾脏Breg细胞亚群占CD19+细胞的比例。结果 实验组心肌炎症水平及CVB3 mRNA表达水平均明显高于对照组;实验组1周亚组心肌组织病理积分低于2周亚组,但实验组1周亚组心肌CVB3 mRNA表达水平却高于2周亚组,差异均有统计学意义(P<0.05)。实验组小鼠脾Breg细胞比例均高于对照组,且实验组1周亚组小鼠脾Breg细胞比例高于2周亚组,差异有统计学意义(P<0.05)。结论 病毒性心肌炎小鼠中调节性B细胞表达增高,其可能参与病毒性心肌炎的发病过程。

关键词: 肠道病毒属, CD19+CD1dhiCD5+ B细胞, 心肌炎, 炎症, 调节性B细胞

Abstract: Objective To observe the changes of regulatory B (Breg) cells in mice with viral myocarditis (VMC) induced by coxsackie virus B3 (CVB3), and to explore the role of Breg cells in VMC mice. Methods Balb/c male mice were randomly divided into experimental group and control group. Mice in the experimental group were intraperitoneally infected with CVB3 to establish VMC models, while mice in the control group were treated with phosphate-buffered saline (PBS) intraperitoneally. According to the time after injection of CVB3 or PBS, all mice in the two groups were randomly divided into 1-week and 2-week subgroups. Myocardial histopathological scores were determined in hematoxylin eosin stained sections. Expression of CVB3 mRNA in heart was measured with real-time reverse transcription-polymerase chain reaction (RT-PCR), and the frequency of splenic Breg subsets in CD19+ B cells was measured with flow cytometry. Results There were significant differences in the pathological scores and expression of myocardial CVB3 mRNA between the VMC mice and controls. The pathological scores of 1-week experimental subgroup were lower than those of 2-week experimental subgroup, while the expression of myocardial CVB3 mRNA in 1-week experimental subgroup was higher than that in 2-week experimental subgroup (all P<0.05). Compared with controls, the frequency of splenic Breg cells in the VMC mice increased significantly at different time points. Moreover, the frequency of splenic Breg cells in 1-week experimental subgroup was higher than that in the 2-week experimental subgroup (all P<0.05). Conclusion Breg cells increase in mice with CVB3-induced VMC, indicating that Breg cells mayplay an important role in the pathogenesis of CVB3-induced VMC.

Key words: Inflammation, Myocarditis, CD19+CD1dhiCD5+ B cells, Enterovirus, Regulatory B cells

中图分类号: 

  • R542.2
[1] Caforio AL, Calabrese F, Angelini A, et al. A prospective study of biopsy-proven myocarditis: prognostic relevance of clinical and aetiopathogenetic features at diagnosis[J]. Eur Heart J, 2007, 28(11):1326-1333.
[2] Sagar S, Liu PP, Cooper LT. Myocarditis[J]. Lancet, 2012, 379(9817): 738-747.
[3] Marchant DJ, Boyd JH, Lin DC, et al. Inflammation in myocardial diseases[J]. Circ Res, 2012, 110(1):126-144.
[4] DiLillo DJ, Matsushita T, Tedder TF. B10 cells and regulatory B cells balance immune responses during inflammation, autoimmunity, and cancer[J]. Ann N Y Acad Sci, 2010, 1183(2010): 38-57.
[5] Yanaba K, Bouaziz JD, Haas KM, et al. A regulatory B cell subset with a unique CD1dhiCD5+ phenotype controls T cell-dependent inflammatory responses[J]. Immunity, 2008, 28(5):639-650.
[6] Yang M, Rui K, Wang S, et al. Regulatory B cells in autoimmune diseases[J]. Cell Mol Immunol, 2013, 10(2):122-132.
[7] 孔清, 高梦莎, 薛贻敏, 等. 白细胞介素-17通过促进巨噬细胞分泌白细胞介素-27参与小鼠病毒性心肌炎的发生[J]. 中华心血管病杂志, 2014, 42(5): 428-432. KONG Qing, GAO Mengsha, XUE Yimin, et al. Interleukin-17 contributes to the macrophage secretion of interleukin-27 in a murine model of viral myocarditis[J]. Chin J Cardiol, 2014, 42(5):428-432.
[8] Candando KM, Lykken JM, Tedder TF. B10 cell regulation of health and disease[J]. Immunol Rev, 2014, 259(1):259-272.
[9] Yanaba K, Bouaziz JD, Matsushita T, et al. The development and function of regulatory B cells expressing IL-10 (B10 cells) requires antigen receptor diversity and TLR signals[J]. J Immunol, 2009, 182(12):7459-7472.
[10] 秦瑶, 张梅, 蒋瑞妹, 等. 小鼠 B10细胞的分离、鉴定及功能特征[J]. 中华微生物学和免疫学杂志, 2013, 33(11): 819-827. QIN Yao, ZHANG Mei, JIANG Ruimei, et al. Isolation, identification and functional characteristics of murine B10 cells[J]. Chin J Microbiol Immunol, 2013, 33(11): 819-827.
[11] 伍昌林, 王前, 郑磊, 等. CITP患者外周血Breg与CD4+T细胞的相关性及临床意义[J]. 中国实验血液学杂志, 2013, 21(6): 1517-1521. WU Changlin, WANG Qian, ZHENG Lei, et al. Correlation of breg with CD4+T Cells of peripheral blood in patients with CITP and its clinical significance[J]. J Exp Hematol, 2013, 21(6): 1517-1521.
[12] Yang M, Deng J, Liu Y, et al. IL-10-producing regulatory B10 cells ameliorate collagen-induced arthritis via suppressing Th17 cell generation[J]. Am J Pathol, 2012, 180(6): 2375-2385.
[13] Matsushita T, Yanaba K, Bouaziz JD, et al. Regulatory B cells inhibit EAE initiation in mice while other B cells promote disease progression[J]. J Clin Invest, 2008, 118(10):3420-3430.
[14] Yang X, Yang J, Chu Y, et al. T follicular helper cells and regulatory B cells dynamics in systemic lupus erythematosus[J]. PLoS One, 2014, 9(2):88441.
[15] Shi L, Bi M, Yang R, et al. Defective expression of regulatory B cells in iodine-induced autoimmune thyroiditis in non-obese diabetic H-2(h4) mice[J]. J Endocrinol Invest, 2014, 37(1):43-50.
[16] Sheng JR, Quan S, Soliven B. CD1d(hi)CD5+ B Cells expanded by GM-CSF in vivo suppress experimental autoimmune myasthenia gravis[J]. J Immunol, 2014, 193(6):2669-2677.
[1] 徐宁宇 王磊 郝恩魁 苏国海. STEMI患者急诊PCI前口服阿托伐他汀对炎症介质及左心室功能的影响[J]. 山东大学学报(医学版), 2209, 47(6): 69-72.
[2] 郝跃伟 刘雪平 赵婷婷 郑敏 王一兵. 环氧化酶2基因多态性与动脉粥样硬化缺血性脑卒中的相关性[J]. 山东大学学报(医学版), 2209, 47(6): 95-98.
[3] 赵灿斌,邵将,管东辉,秦英,丁强,郭良,王伟伟,陈威,闫小龙,曾平. 木犀草素在炎症微环境下调控Wnt/β-catenin信号通路促进骨髓间充质干细胞成软骨分化的机制[J]. 山东大学学报 (医学版), 2025, 63(7): 11-22.
[4] 贾若曦,吕丽,刘涵云,吴寅平,李凤彩,赵泽华,王凯,范玉琛. 血细胞计数相关标志物对慢加急性乙型肝炎肝衰竭患者28天预后的诊断价值[J]. 山东大学学报 (医学版), 2025, 63(6): 89-99.
[5] 张舒淇,江延姣,印丹. 生殖道微生物与子宫内膜异位症发展之间的联系[J]. 山东大学学报 (医学版), 2025, 63(5): 120-126.
[6] 杜艾家,张曼,陈鹤,王丽新,尚应殊. 微小RNA-1270靶向调控血管生成素样蛋白7抑制巨噬细胞炎症和脂质蓄积[J]. 山东大学学报 (医学版), 2025, 63(2): 1-9.
[7] 徐萍,张信美. 子宫内膜异位症疼痛的机制[J]. 山东大学学报 (医学版), 2025, 63(10): 1-7.
[8] 梁炎春,严莹,麦华希,姚书忠. 地诺孕素在子宫内膜异位症相关性疼痛中的治疗作用:从基础到临床[J]. 山东大学学报 (医学版), 2025, 63(10): 27-33.
[9] 孙婧,杨瑞敏,王聪,张月,罗兵. 基于术前超声、炎症指标及超声影像组学联合模型预测乳腺癌腋窝淋巴结转移[J]. 山东大学学报 (医学版), 2025, 63(1): 73-80.
[10] 刘绍庭,张薇薇,冉茜,王建. 食品乳化剂与肠道健康[J]. 山东大学学报 (医学版), 2024, 62(8): 18-26.
[11] 孙丽娜,白红艳,牛宗格,张福帅,曲仪庆. 基于SII构建及评价预测ARDS住院死亡率的在线临床风险模型[J]. 山东大学学报 (医学版), 2024, 62(7): 10-20.
[12] 田丽君,桑玉洁,孙瑜婧,韩冰,秦成勇,祁建妮. 全身免疫炎症指数对原发性肝癌患者免疫检查点抑制剂治疗相关不良反应的预测价值[J]. 山东大学学报 (医学版), 2024, 62(6): 48-53.
[13] 沈海涛,乔亚琴,董萍,路燕. Toll样受体4调控的程序性坏死和铁死亡对对乙酰氨基酚肝损伤的影响[J]. 山东大学学报 (医学版), 2024, 62(4): 1-8.
[14] 徐新军,邵丽婷,陈颖,刘会芳,杨玉娟,张宇,王浛睿,宋西成. SYN008与Xolair®对过敏性哮喘小鼠治疗作用效果比较:炎症与重塑[J]. 山东大学学报 (医学版), 2024, 62(12): 1-10.
[15] 牛雅文,李凤娇. PAR-2在烟曲霉菌感染的人角膜上皮细胞中的作用[J]. 山东大学学报 (医学版), 2024, 62(12): 96-101.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!